Kallmann syndrome: a case of hypogonadotropic hypogonadism.

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dc.contributor.authorSiddiqui, M Nazrul Islamen_US
dc.contributor.authorMia, M Abdur Razzaqueen_US
dc.contributor.authorGhani, M Aen_US
dc.date.accessioned2002-01-01en_US
dc.date.accessioned2009-05-27T03:52:40Z
dc.date.available2002-01-01en_US
dc.date.available2009-05-27T03:52:40Z
dc.date.issued2002-01-01en_US
dc.descriptionMymensingh Medical Journal.en_US
dc.description.abstractAn eighteen years old boy hailing from Nandail, Mymensingh was complaining of small external genitalia, small testes, and gradual enlargement of breast, weight gain, absence of facial, axillary and public hair, absence of sense of smell. His height was 162 cm, weight 59 kg, BMI-22.52 kg/m2 with eunuchoid body habitus. His stretch penile length was 5 cm, testicular volume < 5 ml, stage B3 development of breast and absence of facial, axillary and public hair. He was found anosmic of standard odors. Patient was clinically and biochemically in euthyroid state with low level of testosterone, LH and FSH and normal serum prolactin level. He was diagnosed as a case of hypogonadotropic hypogonadism due to Kallmann syndrome.en_US
dc.description.affiliationDepartment of Endocrinology & Metabolism, MMC, Mymensingh.en_US
dc.identifier.citationSiddiqui MN, Mia MA, Ghani MA. Kallmann syndrome: a case of hypogonadotropic hypogonadism. Mymensingh Medical Journal. 2002 Jan; 11(1): 42-3en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/1081
dc.language.isoengen_US
dc.subject.meshAdolescenten_US
dc.subject.meshHumansen_US
dc.subject.meshHypogonadism --etiologyen_US
dc.subject.meshKallmann Syndrome --complicationsen_US
dc.subject.meshMaleen_US
dc.subject.meshPhenotypeen_US
dc.subject.meshSex Characteristicsen_US
dc.titleKallmann syndrome: a case of hypogonadotropic hypogonadism.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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